RepoSheet™ Original lift aid 3687701Recalls & reported problems
Liko AB · Patient lifting system stretcher · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887761984325), received between May 6, 2026 and May 6, 2026 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 6, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT DEVELOPED LINEAR ULCERS DUE TO THE STRAPS ON THE REPOSHEET. THE REPOSHEET WAS USED TO BOOST THE PATIENT UP IN BED AND IT WAS USED IN THE COURSE OF THEIR STAY. THE PATIENT WAS FOUND TO HAVE SEVERAL AREAS WITH DEEP PURPLE LINEAR DISCOLORATION, ONE OF WHICH DETERIORATED TO A FULL THICKNESS WOUND. THE FACILITIES WOUND OSTOMY TEAM FOLLOWED UP THE PATIENT, THE REPOSHEET WAS REMOVED, AND THE LINEAR DISCOLORATION BEGAN RESOLVING. THE FULL THICKNESS WOUND IS BEING TREATED WITH AQUACEL AG ROPE COVERED WITH MEPILEX. THE DEVELOPMENT OF PRESSURE INJURIES IS MULTIFACTORIAL AND CANNOT ONLY BE ATTRIBUTED TO THE REPOSHEET. ADDITIONALLY THERE IS NO SPECIFIC REPORT OF A DEVICE MALFUNCTION. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Unspecified Tissue Injury
MAUDE report 25094011 ↗
Other Lift, patient, non-ac-powered devices
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- Medline MDS600ELBMedline Industries, Inc. · Lift, patient, non-ac-powered82 reports
- Likorall™ overhead lift 3123001Liko AB · Lift, patient, non-ac-powered1 recall1 death32 reports
- Medline MDS400ELBMedline Industries, Inc. · Lift, patient, non-ac-powered79 reports
- MEDLINE MDS88200HLMedline Industries, Inc. · Lift, patient, non-ac-powered77 reports
- Likorall™ overhead lift 3121001Liko AB · Lift, patient, non-ac-powered1 recall24 reports
- Likorall™ overhead lift 3124050Liko AB · Lift, patient, non-ac-powered1 recall18 reports
- Viking™ XL mobile lift 2040043Liko AB · Lift, patient, non-ac-powered1 recall14 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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